NDC 68071-3259

Prochlorperazine

Prochlorperazine

Prochlorperazine is a Rectal Suppository in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals, Inc.. The primary component is Prochlorperazine.

• Product ID: 68071-3259_50217b0f-a6e4-6c82-e054-00144ff88e88
• NDC: 68071-3259
• Product Type: Human Prescription Drug
• Proprietary Name: Prochlorperazine
• Generic Name: Prochlorperazine
• Dosage Form: Suppository
• Route of Administration: RECTAL
• Marketing Start Date: 1993-11-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA040058
• Labeler Name: NuCare Pharmaceuticals, Inc.
• Substance Name: PROCHLORPERAZINE
• Active Ingredient Strength: 25 mg/1
• Pharm Classes: Phenothiazine [EPC],Phenothiazines [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68071-3259-2

2 SUPPOSITORY in 1 BOTTLE (68071-3259-2)

• Marketing Start Date: 2017-05-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68071-3259-1 [68071325901]

Prochlorperazine SUPPOSITORY

• Marketing Category: ANDA
• Application Number: ANDA040058
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-05-22
• Marketing End Date: 2019-12-31

NDC 68071-3259-2 [68071325902]

Prochlorperazine SUPPOSITORY

• Marketing Category: ANDA
• Application Number: ANDA040058
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-05-22
• Marketing End Date: 2019-12-31

NDC 68071-3259-3 [68071325903]

Prochlorperazine SUPPOSITORY

• Marketing Category: ANDA
• Application Number: ANDA040058
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-05-22
• Marketing End Date: 2019-12-31

NDC 68071-3259-6 [68071325906]

Prochlorperazine SUPPOSITORY

• Marketing Category: ANDA
• Application Number: ANDA040058
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-05-22
• Marketing End Date: 2019-12-31

Drug Details

Active Ingredients

Ingredient	Strength
PROCHLORPERAZINE	25 mg/1

OpenFDA Data

• SPL SET ID: 502148e7-1109-64fd-e054-00144ff88e88
• Manufacturer:
  • NuCare Pharmaceuticals, Inc.
• UNII:
  • YHP6YLT61T
• RxNorm Concept Unique ID - RxCUI:
  • 198159

Pharmacological Class

• Phenothiazine [EPC]
• Phenothiazines [CS]
• Phenothiazine [EPC]
• Phenothiazines [CS]

NDC Crossover Matching brand name "Prochlorperazine" or generic name "Prochlorperazine"

NDC	Brand Name	Generic Name
0713-0135	Prochlorperazine	Prochlorperazine
50090-0636	Prochlorperazine	Prochlorperazine
54348-114	PROCHLORPERAZINE	PROCHLORPERAZINE
54348-989	Prochlorperazine	PROCHLORPERAZINE
66267-176	Prochlorperazine	Prochlorperazine
68071-3259	Prochlorperazine	Prochlorperazine
66213-200	Compazine	Prochlorperazine
0574-7226	Compro	PROCHLORPERAZINE
50090-2881	Compro	PROCHLORPERAZINE
55289-119	Compro	PROCHLORPERAZINE
63629-8444	Compro	PROCHLORPERAZINE